首页> 外文期刊>Virus Research: An International Journal of Molecular and Cellular Virology >The spheroidin of an entomopoxvirus isolated from the grasshopper Anacridium aegyptium (AaEPV) shares low homology with spheroidins from lepidopteran or coleopteran EPVs.
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The spheroidin of an entomopoxvirus isolated from the grasshopper Anacridium aegyptium (AaEPV) shares low homology with spheroidins from lepidopteran or coleopteran EPVs.

机译:从蝗虫埃及cri虫(AaEPV)分离的昆虫痘病毒的球蛋白与来自鳞翅目或鞘翅目EPV的球蛋白具有低同源性。

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摘要

Based on virion morphology, the current virus taxonomy groups entomopoxviruses (EPVs) (Poxvirus: Entomopoxvirinae) from coleopteran and dipteran hosts in separated genera, wilts it keeps viruses infecting either lepidopteran or orthopteran hosts in the same genus. In contrast to the morphological criteria, the few data available from recent studies at the genetic level have suggested that EPVs infecting different insect orders are phylogenetically distant. In order to elucidate EPVs phylogeny we have cloned and sequence the highly conserved/highly expressed spheroidin gene of Anacridium aegyptium entomopoxvirus (AaEPV). This gene and its promoter is of interest for the development of genetic engineering on EPVs. The spheroidin gene was located in the AaEPV genome by Southern blot and hybridisation with specific degenerated oligonucleotides probes synthesised after partial sequencing of the purified spheroidin protein. A total of 3489 bp were sequenced. This sequence included the coding and promoter region of 969 residues 108. 8 kDa protein identified as spheroidin. AaEPV spheroidin contains 21 cysteine residues (2.2%) and 14 N-glycosylation putative sites distributed along the sequence. The cysteine residues are particularly abundant at the C-terminal end of the protein, with 11 residues in the last 118 aa. Our results confirm that the spheroidin is highly conserved only between EPVs isolated from the same insect order. Polyclonal antibodies raised against AaEPV spherules specifically revealed spheroidin in Western Blots failing to cross-react with MmEPV or AmEPV spheroidins or MmEPV fusolin. Comparison of spheroidins at the aa level demonstrate that AaEPV spheroidin shares only 22.2 and 21.9% identity with the lepidopteran AmEPV and the coleopteran MmEPV spheroidins, respectively, but 82.8% identity with the orthopteran MsEPV spheroidin. Only two highly conserved domains containing the sequence (V/Y)NADTG(C/L) and LFAR(I/A) have been identified in all known spheroidins. The phylogenetic tree constructed according to the CLUSTALX analysis program revealed that EPVs are clearly separated in three groups - lepidopteran, coleopteran and orthopteran - according to the insect order of the virus hosts. In base to our results, the split of the genus Entomopoxvirus B dissociating lepidopteran and orthopteran EPVs into two different genera is suggested.
机译:基于病毒体形态,当前的病毒分类法将分离的属中的鞘翅目和双翅目宿主的昆虫痘病毒(EPV)(Poxvirus:Entomopoxvirinae)进行分组,以使其保持感染同一属的鳞翅目或直翅目宿主的病毒。与形态学标准相反,最新的遗传学研究数据很少表明,感染不同昆虫纲的EPV在系统发育上相距遥远。为了阐明EPV的系统发育,我们已经克隆并测序了高度保守/高表达的Anacridium aegyptium entomopoxvirus(AaEPV)球蛋白基因。该基因及其启动子对于在EPV上进行基因工程的开发很感兴趣。通过Southern印迹将球蛋白基因定位在AaEPV基因组中,并与对纯化的球蛋白蛋白质进行部分测序后合成的特定变性寡核苷酸探针杂交。总共测序了3489 bp。该序列包括969个残基108的编码和启动子区域。鉴定为spheroidin的8kDa蛋白。 AaEPV球蛋白包含21个半胱氨酸残基(2.2%)和14个沿序列分布的N-糖基化推定位点。半胱氨酸残基在蛋白质的C末端特别丰富,在最后的118个氨基酸中有11个残基。我们的结果证实,球蛋白仅在从相同昆虫纲中分离的EPV之间是高度保守的。针对AaEPV小球产生的多克隆抗体在Western Blot中特异显示了Spheroidin,无法与MmEPV或AmEPV Spheroidins或MmEPV Fusolin交叉反应。在aa水平上对球蛋白的比较表明,AaEPV球蛋白分别与鳞翅目AmEPV和鞘翅目MmEPV球蛋白分别具有22.2和21.9%的同一性,但与直翅目MsEPV球蛋白具有82.8%的同一性。在所有已知的椭球蛋白中,仅鉴定出两个高度保守的包含序列(V / Y)NADTG(C / L)和LFAR(I / A)的域。根据CLUSTALX分析程序构建的系统发育树显示,根据病毒宿主的昆虫顺序,EPV清楚地分为鳞翅目,鞘翅目和直翅目三类。根据我们的研究结果,建议将昆虫鳞茎乙病毒分开,将鳞翅目和直翅目EPV分离为两个不同的属。

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